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rs119488100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119488100(A;A)
Make rs119488100(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93777551
GeneLGI1
is asnp
is mentioned by
dbSNPrs119488100
ebirs119488100
HLIrs119488100
Exacrs119488100
Varsomers119488100
Maprs119488100
PheGenIrs119488100
hapmaprs119488100
1000 genomesrs119488100
hgdprs119488100
ensemblrs119488100
gopubmedrs119488100
geneviewrs119488100
scholarrs119488100
googlers119488100
pharmgkbrs119488100
gwascentralrs119488100
openSNPrs119488100
23andMers119488100
23andMe allrs119488100
SNP Nexus

SNPshotrs119488100
SNPdbers119488100
MSV3drs119488100
GWAS Ctlgrs119488100
Max Magnitude0
OMIM604619
Desc
Variant0011
Relatedalso
ClinVar
Risk rs119488100(A;A)
Alt rs119488100(A;A)
Reference rs119488100(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95537308T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005772.2,